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Letter to the Editor Regarding “Impact of Vaginal-Rectal Ultrasound Examinations with Covered and Low-Level Disinfected Transducers on Infectious Transmissions in France” by Leroy et al.

Published online by Cambridge University Press:  23 April 2015

Thomas Bénet
Affiliation:
Infection Control and Epidemiology Unit, Hospices Civils de Lyon, Lyon, France Biometry and Evolutive Biology Laboratory, Biostatistics and Health Unit, Lyon 1 University, and National Center for Scientific Research, Mixed Research Unit 5558, Villeurbanne, and Lyon 1 University, Lyon, France
René Ecochard
Affiliation:
Biometry and Evolutive Biology Laboratory, Biostatistics and Health Unit, Lyon 1 University, and National Center for Scientific Research, Mixed Research Unit 5558, Villeurbanne, and Lyon 1 University, Lyon, France Department of Biostatistics, Lyon University Hospitals, Lyon, France.
Philippe Vanhems*
Affiliation:
Infection Control and Epidemiology Unit, Hospices Civils de Lyon, Lyon, France Biometry and Evolutive Biology Laboratory, Biostatistics and Health Unit, Lyon 1 University, and National Center for Scientific Research, Mixed Research Unit 5558, Villeurbanne, and Lyon 1 University, Lyon, France
*
Address correspondence to Philippe Vanhems, MD, PhD, Service d’Hygiène, Epidémiologie et Prévention, Hôpital Edouard Herriot, Hospices Civils de Lyon, 5 place d’Arsonval, 69437 Lyon CEDEX 03, France (philippe.vanhems@chu-lyon.fr).
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Abstract

Type
Letters to the Editor
Copyright
© 2015 by The Society for Healthcare Epidemiology of America. All rights reserved 

To the Editor—A simulation study on the impact of vaginal-rectal ultrasound examinations on infectious risks in France was published recently by Leroy and colleagues.Reference Leroy, M’Zali, Kann, Weber and Smith 1 Although statistical methods with Monte Carlo simulations could be contributive, we would like to raise some points which might limit the interpretation of their results.

The uncertainty of several parameters was possibly very wide, and simulation did not take such variability into account. The probability that a pathogen lingered on the probe after cleaning and disinfection was derived from data on bacterial agents in 2 single-center studies,Reference Kac, Podglajen, Si-Mohamed, Rodi, Grataloup and Meyer 2 , Reference Kac, Gueneret and Rodi 3 whereas most infections simulated by Leroy et al were viral. The probability of probe contamination from an infected patient was extracted from observational data on sexual intercourse. However, the probability of transmission differed according to type of sexual intercourse, inoculum or viral load.Reference Hughes, Baeten and Lingappa 4 Sexual exposure was most probably very dissimilar from endocavitary ultrasound exposure. With hepatitis C virus, the rate of transmission differed strongly between infection observed among drug usersReference Thorpe, Ouellet and Hershow 5 and patients after nosocomial exposure, such as hemodialysis.Reference Petrosillo, Gilli and Serraino 6 Similarly, with human immunodeficiency virus, the probability of infection after accidental bloodReference Henderson, Fahey and Willy 7 and male-to-female sexual exposuresReference Hughes, Baeten and Lingappa 4 is distinct with 0.003 and 0.0019 probability densities, respectively. Sensitivity analyses should have been conducted to properly interpret the results.

In a hypothetical cohort of 4 million exposed patients in France,Reference Leroy, M’Zali, Kann, Weber and Smith 1 the authors ascertained that a mean (SD) of 40 (20) would be infected by human immunodeficiency virus and 151 (63) by hepatitis C virus annually. Recently, our group studied a French prospective, observational, hospital-based cohort of 16,474 individualsReference Bénet, Ritter and Vanhems 8 and found that the incidence of human immunodeficiency virus seroconversion was 0 (n=0) per 10,000 patient-years in patients with endocavitary probe exposure within 12 months before testing and 6.7 (n=13) in nonexposed patients (log-rank test: P=.64). The incidence of hepatitis C virus seroconversion was 16.1 (n=1) per 10,000 patient-years in patients exposed to endocavitary probes and 23.4 in nonexposed patients (log-rank test: P=.69).

In a letter published elsewhere,Reference Bénet and Vanhems 9 our group underlined that statistical analysis of a previous meta-analysis by Leroy,Reference Leroy 10 based on 2 published studies, would be questionable owing to lack of weighting according to study size. However, similar data were analyzed, again with a dearth of details regarding the calculation of pooled prevalence.Reference Henderson, Fahey and Willy 7 We agree with Leroy et alReference Leroy, M’Zali, Kann, Weber and Smith 1 that the issue of probe contamination is important and could be a public health concern, particularly with human papillomavirus infection related to endocavitary ultrasound exposure. Additional sensitivity analysis would have improved the accuracy of estimations in the present study.Reference Leroy, M’Zali, Kann, Weber and Smith 1 Appropriate prospective investigations are needed with a view to proposing the best preventive measures for patient safety regarding these exposures.

Acknowledgments

Financial support. None reported.

Potential conflicts of interest. All authors report no conflicts of interest relevant to this article.

References

1. Leroy, S, M’Zali, F, Kann, M, Weber, DJ, Smith, DD. Impact of vaginal-rectal ultrasound examinations with covered and low-level disinfected transducers on infectious transmissions in France. Infect Control Hosp Epidemiol 2014;35:14971504.CrossRefGoogle ScholarPubMed
2. Kac, G, Podglajen, I, Si-Mohamed, A, Rodi, A, Grataloup, C, Meyer, G. Evaluation of ultraviolet C for disinfection of endocavitary ultrasound transducers persistently contaminated despite probe covers. Infect Control Hosp Epidemiol 2010;31:165170.CrossRefGoogle ScholarPubMed
3. Kac, G, Gueneret, M, Rodi, A, et al. Evaluation of a new disinfection procedure for ultrasound probes using ultraviolet light. J Hosp Infect 2007;65:163168.Google Scholar
4. Hughes, JP, Baeten, JM, Lingappa, JR, et al; Partners in Prevention HSV/HIV Transmission Study Team. Determinants of per-coital-act HIV-1 infectivity among African HIV-1-serodiscordant couples. J Infect Dis 2012;205:358365.Google Scholar
5. Thorpe, LE, Ouellet, LJ, Hershow, R, et al. Risk of hepatitis C virus infection among young adult injection drug users who share injection equipment. Am J Epidemiol 2002;155:645653.Google Scholar
6. Petrosillo, N, Gilli, P, Serraino, D, et al. Prevalence of infected patients and understaffing have a role in hepatitis C virus transmission in dialysis. Am J Kidney Dis 2001;37:10041010.CrossRefGoogle ScholarPubMed
7. Henderson, DK, Fahey, BJ, Willy, M, et al. Risk for occupational transmission of human immunodeficiency virus type 1 (HIV-1) associated with clinical exposures: a prospective evaluation. Ann Intern Med 1990;113:740746.Google Scholar
8. Bénet, T, Ritter, J, Vanhems, P. Risk of human immunodeficiency virus and hepatitis C virus infection related to endocavitary ultrasound probe exposure in France. Infect Control Hosp Epidemiol 2014;35:14291431.Google Scholar
9. Bénet, T, Vanhems, P. Methodological issues concerning the meta-analysis by Leroy on the risk of infectious complications after endovaginal and transrectal ultrasonography. J Hosp Infect 2014;88:5253.Google Scholar
10. Leroy, S. Infectious risk of endovaginal and transrectal ultrasonography: systematic review and meta-analysis. J Hosp Infect 2013;83:99106.Google Scholar